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Items: 1 to 20 of 169

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112778copy number variation1nstd102humanPathogenic GRCh37 chr20: 51,799,648-62,916,626 , GRCh38.p12 chr20: 53,183,109-64,285,273 LINC01742, MTCO2P1, 253 more genes
    nsv5730403mobile element insertion1nstd211human GRCh38 chr20: 62,140,671-62,140,671 , GRCh37.p13 chr20: 60,715,727-60,715,727 PSMA7
    nsv5289201copy number variation1nstd204human GRCh38.p13 chr20: 62,058,601-62,909,300 , GRCh37.p13 chr20: 60,633,657-61,540,652 , LOC105372716, 47 more genes
    nsv5284819copy number variation1nstd204human GRCh38.p13 chr20: 62,134,401-62,423,600 , GRCh37.p13 chr20: 60,709,457-60,998,656 , RPS21, 15 more genes
    nsv5022528copy number variation1nstd200human GRCh38 chr20: 62,143,645-62,143,900 , GRCh37.p13 chr20: 60,718,701-60,718,956 SS18L1, PSMA7
    nsv4680664copy number variation1nstd189human GRCh37.p13 chr20: 60,162,844-60,832,983 , GRCh38.p12 chr20: 61,587,788-62,257,927 CDH4, PSMA7, 14 more genes
    nsv4676332copy number variation1nstd102humanPathogenic GRCh37 chr20: 55,743,522-62,032,989 , GRCh38.p12 chr20: 57,168,466-63,401,636 BMP7, MIR298, 153 more genes
    nsv4676181copy number variation1nstd102humanPathogenic GRCh37 chr20: 56,788,101-62,762,405 , GRCh38.p12 chr20: 58,213,045-64,131,052 LOC105372697, MIR647, 174 more genes
    nsv4673689copy number variation1nstd186human GRCh37 chr20: 60,718,240-60,718,341 , GRCh38.p12 chr20: 62,143,184-62,143,285 SS18L1, PSMA7
    nsv4632530copy number variation1nstd183human GRCh37 chr20: 60,718,405-60,719,511 , GRCh38.p12 chr20: 62,143,349-62,144,455 SS18L1, PSMA7
    nsv4628358copy number variation1nstd183human GRCh37 chr20: 60,717,607-60,718,317 , GRCh38.p12 chr20: 62,142,551-62,143,261 SS18L1, PSMA7
    nsv4626324copy number variation1nstd183human GRCh37 chr20: 60,717,660-60,718,317 , GRCh38.p12 chr20: 62,142,604-62,143,261 PSMA7, SS18L1
    nsv4621314copy number variation1nstd183human GRCh37 chr20: 60,718,240-60,718,341 , GRCh38.p12 chr20: 62,143,184-62,143,285 SS18L1, PSMA7
    nsv4422177copy number variation1nstd174human GRCh37 chr20: 60,718,405-60,719,511 , GRCh38.p12 chr20: 62,143,349-62,144,455 SS18L1, PSMA7
    nsv4357849copy number variation1nstd102humanPathogenic GRCh37 chr20: 54,143,747-62,194,881 , GRCh38.p12 chr20: 55,568,689-63,563,528 RBM38, LAMA5, 192 more genes
    nsv4315247insertion1nstd166human GRCh37.p13 chr20: 60,717,818-60,717,818 , GRCh38.p12 chr20: 62,142,762-62,142,762 PSMA7, SS18L1
    nsv3924938copy number variation1nstd102humanUncertain significance GRCh38 chr20: 61,588,953-62,241,744 , NCBI36 chr20: 59,597,404-60,250,195 , GRCh37 chr20: 60,164,009-60,816,800 LOC105372705, MIR3195, 14 more genes
    nsv3924353copy number variation1nstd102humanPathogenic NCBI36 chr20: 59,335,000-62,379,123 , GRCh38 chr20: 61,326,549-64,277,326 , GRCh37 chr20: 59,901,605-62,908,679 PPDPF, CRMA, 126 more genes
    nsv3920218copy number variation1nstd102humanPathogenic GRCh37 chr20: 80,198-62,908,674 , GRCh38 chr20: 99,557-64,277,321 , NCBI36 chr20: 28,198-62,379,118 MIR3646, NPEPL1, 1310 more genes
    nsv3916789copy number variation1nstd102humanPathogenic GRCh37 chr20: 57,617,021-62,908,674 , GRCh38 chr20: 59,041,966-64,277,321 , NCBI36 chr20: 57,050,416-62,379,118 RNU7-141P, UCKL1, 153 more genes
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